Wu Mu-Lu, Chan Chuu Ling, Dick Thomas
Antibacterial Drug Discovery Laboratory, Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore Singapore, Singapore.
Front Microbiol. 2016 Aug 31;7:1390. doi: 10.3389/fmicb.2016.01390. eCollection 2016.
Recently we showed that upon transfer of growing Mycobacterium smegmatis into saline, the bacilli exited the canonical cell division cycle and formed septated multi-nucleoided cells. Under shock starvation (i.e., in saline without any carbon source), differentiation terminated at this stage with internally remodeled Large Resting Cells (LARCs). Whereas under gentle starvation (i.e., in saline with trace amounts of a carbon source), the septated multi-nucleoided bacilli completed cell division and separated into mono-nucleoided Small Resting Cells (SMRCs). This demonstrated that the non-sporulating mycobacteria are in fact capable of forming morphologically differentiated resting cells when exposed to starvation. Depending on the specific starvation conditions they can form two different resting cell types, LARCs or SMRCs, which share a common cellular differentiation pathway. The mRNA encoding the (p)ppGpp synthetase Rel was found to be transiently upregulated immediately upon starvation under both conditions, suggesting a role for the stringent response factor in both LARC and SMRC development. Here, we disrupted Rel function by generating two types of mutant M. smegmatis strains: a rel nonsense mutant (rel (E4TAG)) in which translation is prematurely terminated at codon 4, and a rel deletion mutant (Δrel) in which the entire coding sequence was deleted. Both mutants showed identical phenotypes: sparse septum formation, less DNA compaction, and failure in formation of both the septated multi-nucleoided LARCs and the small-cell morphotype SMRC under starvation conditions. All phenotypes were rescued through the introduction of a wild-type copy of rel. Therefore, we conclude that loss-of-function mutations in rel block the development of both LARCs and SMRCs by preventing the first morphogenetic step in mycobacterial resting cell development, the formation of septated multi-nucleoided cells. Interestingly, in contrast to Rel's role in most other bacteria, starvation survival was not affected by loss of rel function. Our results suggest that Rel may play a starvation-induced morphogenetic role in mycobacteria.
最近我们发现,将生长中的耻垢分枝杆菌转移至盐溶液中后,杆菌退出经典的细胞分裂周期,形成具有隔膜的多核细胞。在休克饥饿状态下(即处于无任何碳源的盐溶液中),分化在这一阶段终止,形成内部重塑的大型静止细胞(LARC)。而在轻度饥饿状态下(即处于含有微量碳源的盐溶液中),具有隔膜的多核杆菌完成细胞分裂,分离成单核的小型静止细胞(SMRC)。这表明,非产孢分枝杆菌在暴露于饥饿状态时实际上能够形成形态分化的静止细胞。根据特定的饥饿条件,它们可以形成两种不同的静止细胞类型,LARC或SMRC,它们共享一条共同的细胞分化途径。发现在两种条件下饥饿后,编码(p)ppGpp合成酶Rel的mRNA会立即短暂上调,这表明严格反应因子在LARC和SMRC的发育中均发挥作用。在此,我们通过构建两种耻垢分枝杆菌突变株来破坏Rel的功能:一种是rel无义突变株(rel(E4TAG)),其翻译在第4密码子处提前终止;另一种是rel缺失突变株(Δrel),其整个编码序列被删除。两种突变株表现出相同的表型:隔膜形成稀疏、DNA压缩程度降低,并且在饥饿条件下无法形成具有隔膜的多核LARC和小细胞形态型SMRC。通过引入rel的野生型拷贝,所有表型均得到挽救。因此,我们得出结论,rel的功能丧失突变通过阻止分枝杆菌静止细胞发育中的第一步形态发生,即具有隔膜的多核细胞的形成,从而阻碍了LARC和SMRC的发育。有趣的是,与Rel在大多数其他细菌中的作用不同,rel功能丧失并不影响饥饿存活。我们的结果表明,Rel可能在分枝杆菌中发挥饥饿诱导的形态发生作用。